EUA

Rapid SARS-CoV-2 Antigen Test Card

FDA Emergency Use Authorization · Xiamen Boson Biotech Co., Ltd. · Jan 23, 2024

Key facts

Product Rapid SARS-CoV-2 Antigen Test Card
Company Xiamen Boson Biotech Co., Ltd.
Product type Lateral Flow, Visual Read, Over the Counter (OTC) Home Testing, Serial Testing, Serial Screening, Single Target
Date Jan 23, 2024
FDA page fda.gov

At a glance

  • 10–99 Authorization documents
  • 1–9 EUAs for this company

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Emergency Use Authorizations

Emergency Use Authorizations allow the FDA to permit unapproved medical products, or unapproved uses of approved products, during a declared public health emergency.

Source: U.S. Food and Drug Administration (FDA), Emergency Use Authorizations · Source date:

Browse all Emergency Use Authorizations